Chromium picolinate compositions and uses thereof

ABSTRACT

Compositions comprising chromic tripicolinate or chromic polynicotinate in combination with at least one of a cyclooxygenase inhibitor, an acid, a mucolytic and a salicin-containing herb. The compositions are useful for supplementing dietary chromium, lowering blood glucose levels, lowering serum lipid levels and increasing lean body mass.

RELATED APPLICATION

This application is a continuation of application Ser. No. 09/291,561,filed Apr. 14, 1999, now U.S. Pat. No. 6,143,301, which is acontinuation-in-part of U.S. application Ser. Nos. 09/228,701, filedJan. 12, 1999, now U.S. Pat. No. 6,093,711, and Ser. No. 09/144,026,filed Aug. 28, 1998, now U.S. Pat. No. 5,948,772 the entire contents ofwhich are hereby incorporated by reference.

FIELD OF THE INVENTION

The present invention relates to compositions comprising chromictripicolinate or chromic polynicotinate in combination with at least oneof a cyclooxygenase inhibitor, acid, mucolytic and salicin-containingherb, and uses of these compositions in lowering blood glucose levels,increasing lean body mass and lowering blood serum lipid levels.

BACKGROUND OF THE INVENTION

Chromium is a nutritionally essential trace element. The essentiality ofchromium in the diet was established in 1959 by Schwartz, as cited inPresent Knowledge in Nutrition, page 571, fifth edition (1984, theNutrition Foundation, Washington, DC). Chromium depletion ischaracterized by the disturbance of glucose, lipid and proteinmetabolism and by a shortened lifespan. Chromium is essential foroptimal insulin activity in all known insulin-dependent systems (Boyleet al., Southern Med. J. 70:1449-1453, 1977). Insufficient dietarychromium has been linked to both maturity-onset diabetes and tocardiovascular disease.

The principle energy sources for the body are glucose and fatty acids.Chromium depletion results in biologically ineffective insulin andcompromised glucose metabolism. Under these conditions, the body mustrely primarily on lipid metabolism to meet its energy requirements,resulting in the production of excessive amounts of acetyl-CoA andketone bodies. Some of the documented acetyl-CoA is converted toincreased cholesterol biosynthesis, resulting in hypercholesterolemia.Diabetes mellitus is characterized in large part by glycosuria,hypercholesterolemia, and often ketoacidosis. The acceleratedatherosclerotic process seen in diabetics is associated withhypercholesterolemia (Boyle et al., supra).

Dietary supplementation of chromium to normal individuals has beenreported to lead to improvements in glucose tolerance, serum lipidconcentrations, including high-density lipoprotein cholesterol, insulinand insulin binding (Anderson, Clin. Psychol. Biochem. 4:31-41, 1986).Supplemental chromium in the trivalent form, e.g. chromic chloride, isassociated with improvements of risk factors associated with adult-onset(Type II) diabetes and cardiovascular disease.

Chromium functions as a cofactor for insulin. It binds to the insulinreceptor and potentiates many, and perhaps all, of its functions (Boyleet al., supra.). These functions include, but are not limited to, theregulation of carbohydrate and lipid metabolism. (Present Knowledge inNutrition, supra, at p. 573-577). The introduction of inorganic chromiumcompounds per se into individuals is not particularly beneficial.Chromium must be converted endogenously into an organic complex or mustbe consumed as a biologically active molecule. Only about 0.5% ofingested inorganic chromium is assimilated into the body (RecommendedDaily Allowances, Ninth Revised Edition, The National Academy ofSciences, page 160, 1980). Only 1-2% of most organic compounds isassimilated into the body.

U.S. Pat. No. Re. 33,988 discloses that when selected essential metals,including chromium, are administered to mammals as exogenouslysynthesized coordination complexes of picolinic acid, they are directlyavailable for absorption without competition from other metals. Thispatent describes a composition and method for selectively supplementingthe essential metals in the human diet and for facilitating absorptionof these metals by intestinal cells. These complexes are safe,inexpensive, biocompatible and easy to produce. These exogenouslysynthesized essential metal coordination complexes of picolinic acid(pyridine-2-carboxylic acid) have the following structural formula:

wherein M represents the metallic cation and n is equal to the cation'svalence. For example, when M is Cr and n=3, then the compound is chromictripicolinate. Other chromium picolinates disclosed include chromicmonopicolinate and chromic dipicolinate.

The U.S. Recommended Daily Intake (RDI) of chromium is 120 μg. U.S. Pat.No. 5,087,623, the entire contents of which are hereby incorporated byreference, describes the administration of an effective amount ofchromic tripicolinate for the treatment of adult-onset diabetes.International Patent Application No. WO96/35421 discloses the use ofhigh doses of chromic tripicolinate (providing 1,000-10,000 μgchromium/day) for reducing hyperglycemia and stabilizing the level ofserum glucose in humans with Type II diabetes. Allowed U.S. patentapplication Ser. No. 08/908,819 discloses a chromic tripicolinate-biotincomposition and its use in lowering blood glucose levels in humans withType II diabetes.

U.S. Pat. Nos. 5,087,623; 5,087,624; and 5,175,156, the entire contentsof which are hereby incorporated by reference, disclose the use ofchromium tripicolinate for supplementing dietary chromium, reducinghyperglycemia and stabilizing serum glucose, increasing lean body massand reducing body fat, and controlling blood serum lipid levels,including the lowering of undesirably high blood serum LDL-cholesterollevels and the raising of blood serum HDL-cholesterol levels. U.S. Pat.Nos. 4,954,492 and 5,194,615, the entire contents of which are herebyincorporated by reference, describe a related complex, chromicpolynicotinate, which is also used for supplementing dietary chromiumand lowering serum lipid levels. Picolinic acid and nicotinic acid areposition isomers having the following structures:

Nicotinic acid and picolinic acid form coordination complexes withmonovalent, divalent and trivalent metal ions and facilitate theabsorption of these metals by transporting them across intestinal cellsand into the bloodstream. Chromium absorption in rats following oraladministration of CrCl₃ was facilitated by the non-steroidalanti-inflammatory drugs (NSAIDs) aspirin and indomethacin (Davis et al.,J. Nutrition Res. 15:202-210, 1995; Kamath et al., J. Nutrition127:478-482, 1997). These drugs inhibit the enzyme cyclooxygenase whichconverts arachidonic acid to various prostaglandins, resulting ininhibition of intestinal mucus formation and lowering of intestinal pHwhich facilitates chromium absorption.

The present invention provides improved chromic tripicolinate andchromic polynicotinate compositions which facilitate absorption ofchromium and other endogenous or exogenous metals, for use in loweringblood glucose levels, serum lipid levels and increasing lean body mass.

SUMMARY OF THE INVENTION

One embodiment of the present invention is a composition forsupplementing dietary chromium and facilitating absorption of essentialmetals, the composition comprising chromic tripicolinate in combinationwith at least one of a cyclooxygenase inhibitor, an acid, a mucolyticand a salicin-containing herb, wherein the composition is not entericcoated. Preferably, the cyclooxygenase inhibitor is aspirin,indomethacin, ibuprofen, acetaminophen, naproxen or other compound withcyclooxygenase inhibitor activity, e. g. vitamin E. In one aspect ofthis preferred embodiment, the mucolytic is guaifenesin. In anotheraspect of this preferred embodiment, the acid is ascorbic acid or citricacid. Advantageously, the formulation is a tablet, capsule or microbead.Preferably, the microbead is a sugar beadlet or microcrystallinecellulose beadlet and the composition is coated on the beadlet.

The present invention also provides a method for supplementing dietarychromium in an individual, comprising orally administering to theindividual a composition comprising chromic tripicolinate in combinationwith at least one of a cyclooxygenase inhibitor, an acid, a mucolyticand a salicin-containing herb, wherein the composition is not entericcoated. In one aspect of this preferred embodiment, the formulation is atablet, capsule or microbead. Preferably, the microbead is a sugarbeadlet or microcrystalline cellulose beadlet and the composition iscoated on the beadlet.

Another embodiment of the invention is a method for reducinghyperglycemia and stabilizing serum glucose levels in an individual inneed thereof, comprising orally administering to the individual aneffective daily hyperglycemia-reducing amount of a compositioncomprising chromic tripicolinate in combination with at least one of acyclooxygenase inhibitor, an acid, a mucolytic and a salicin-containingherb, wherein the composition is not enteric coated. Advantageously, thecomposition is in the form of a tablet, capsule or microbead. Preferablythe microbead is a sugar beadlet or microcrystalline cellulose beadletand the composition is coated on the beadlet.

Another embodiment of the invention is a method for increasing lean bodymass and reducing body fat of an individual in need thereof, comprisingorally administering to the individual an effective, lean bodymass-increasing amount of a composition comprising chromic tripicolinatein combination with at least one of a cyclooxygenase inhibitor, an acid,a mucolytic and a salicin-containing herb, wherein the composition isnot enteric coated. In one aspect of this preferred embodiment, thecomposition is in the form of a tablet, capsule or microbead.Preferably, the microbead is a sugar beadlet or microcrystallinecellulose beadlet and the composition is coated on the beadlet.

The present invention also provides a method for reducing high levels ofblood serum lipids in an individual in need thereof, comprisingadministering to the individual an effective blood serum lipid-reducingamount of a composition comprising chromic tripicolinate in combinationwith at least one of a cyclooxygenase inhibitor, an acid, a mucolyticand a salicin-containing herb, wherein the composition is not entericcoated. In one aspect of this preferred embodiment, the composition isin the form of a tablet, capsule or microbead. Preferably, the microbeadis a sugar beadlet or microcrystalline cellulose beadlet and thecomposition is coated on the beadlet.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention provides compositions comprising chromictripicolinate or chromic polynicotinate in combination with at least oneof a cyclooxygenase (cox) inhibitor, acid, mucolytic andsalicin-containing herb. In a preferred embodiment, the chromictripicolinate and chromic polynicotinate are synthetic. The chromictripicolinate and chromic polynicotinate facilitate absorption ofchromium by intestinal cells, while the additional picolinic acid and/ornicotinic acid in the composition facilitates absorption of otheringested chromium as well as other metals including, but not limited to,copper, iron, magnesium, manganese and zinc.

In one embodiment of the invention, the chromic tripicolinate andchromic polynicotinate compositions are coated with an enteric coatingwhich prevents dissolution of the tablet, capsule or microbead in theacidic environment of the stomach. Instead, this coating dissolves inthe small intestine at a more neutral pH. Because chromic tripicolinateand chromic polynicotinate may be more stable at this neutral pH than atthe acidic pH of the stomach, enhanced absorption occurs because thechromic tripicolinate and chromic polynicotinate remain substantiallyintact until they reach the small intestine. In addition, becausechromic tripicolinate and chromic polynicotinate bind to food in thestomach which may inhibit their absorption by the small intestine,enteric coatings beneficially delay dissolution until the compoundsreach the small intestine. Such enteric coated compositions aredescribed by Bauer et al., Coated Pharmaceutical Dosage Forms:Fundamentals, Manufacturing Techniques, Biopharmaceutical Aspects, TestMethods and Raw Materials, CRC Press, Washington, D.C., 1998, the entirecontents of which are hereby incorporated by reference.

In another embodiment of the invention, the chromic tripicolinate andchromic polynicotinate compositions are provided in combination with atleast one of a cox inhibitor, acid, mucolytic and salicin-containingherb. Cox inhibitors include, but are not limited to, aspirin(acetylsalicylic acid), other salicylates, or another NSAID such asindomethacin, ibuprofen, acetaminophen, naproxen or any compound capableof inhibiting the cyclooxygenase pathway leading to prostaglandinsynthesis. This results in a decrease in intestinal mucus production andlower intestinal pH which facilitates absorption of the chromictripicolinate compositions of the present invention. The oralcompositions may further include mucolytics such as guaifenesin and thelike, to inhibit intestinal mucus production, and/or acids such asascorbic acid, citric acid and the like to lower intestinal pH.Inclusion of one or both of these compounds further enhances chromiumabsorption. There are two forms of cyclooxygenase (cox), cox1 and cox2,which differ in their sensitivity to inhibition by NSAIDs. The cox2isozyme promotes prostaglandin formation at sites of inflammation, butnot at other sites such as the gastrointestinal tract. In contrast,relatively selective inhibition of cox1 facilitates chromictripicolinate and chromic polynicotinate absorption. Although theselective inhibition of cox1 is desirable, any inhibitor or cox1 or cox2can be formulated with the chromic tripicolinate and chromicpolynicotinate compositions of the invention. Cox inhibitors, acids andmucolytics may also be coadministered with the chromic tripicolinate andchromic polynicotinate compositions of the invention. The amount ofthese drugs formulated with or coadministered with the chromictripicolinate and chromic polynicotinate compositions of the inventionare as follows: cox inhibitors, between about 50 mg and 500 mg;mucolytics, between about 10 mg and 250 mg; and acids, between about 50mg and about 1,000 mg.

The coadministration or formulation of salicylate-containing herbs withthe chromic tripicolinate and chromic polynicotinate compositions of theinvention is also contemplated. Class I herbs, as documented in theAmerican Herbal Products Association's Botanical Safety Handbook (herbsthat can be safely consumed when used appropriately), such as Boswelliaserrata (frankincense), Betula lenta (sweet birch), Betula pubescens(white birch), Filipendula ulmaria (meadowsweet), Gaultheria procumbens(wintergreens), Populus balsamifera and Populus jackii (balm of Gilead),and Salix alba (white willow) are all salicin-containing plants withsalicylate-like properties. These herbs suppress prostaglandin synthesisby cox inhibition, thereby improving absorption of the chromictripicolinate compositions of the invention. These herbs are relativelyfree from gastric ulcerogenic effects (Singh et al., Agents and Actions18:407-412, 1986). In addition, preclinical acute toxicity studies haveshown that salicin-containing plants do not cause hematologicaldisturbances (American Herbal Products Association, Botanical SafetyHandbook, 1997).

The compounds and herbs described above all effect gut physiology byinhibiting prostaglandin synthesis, decreasing mucus production, andlowering gastrointestinal pH. The inclusion of these compounds, as wellas an enteric coating, into the oral chromic tripicolinate and chromicpolynicotinate compositions of the invention results in a multicomponentdelivery system which allows delivery of these agents to thegastrointestinal tract where they work in concert to facilitate chromictripicolinate absorption.

Thus, these compositions are readily absorbable forms of chromium whichalso facilitate absorption of other essential metals in the human diet.The chromic tripicolinate and chromic polynicotinate compositions of theinvention have the same uses as described for chromic tripicolinate inU.S. Pat. Nos. 5,087,623, 5,087,624, and 5,174,156, namely supplementingdietary chromium, lowering blood glucose levels in diabetics, loweringserum lipid levels and increasing lean body mass.

The synthesis and use of chromium picolinates is described in U.S. Pat.Nos. Re 33,988 and 5,087,623. Chromic tripicolinate is available fromhealth food stores, drug stores and other commercial sources, includingNutrition 21 (San Diego, Calif.). The synthesis and use of chromicpolynicotinate is described in U.S. Pat. No. 5,194,615. Picolinic acidand nicotinic acid are available from many commercial sources, includingSigma-Aldrich (St. Louis, Mo.) (picolinic acid; catalog No. P5503;nicotinic acid; catalog No. PN4126). The compositions of the presentinvention are prepared by incorporating the components into apharmaceutically acceptable carrier, including but not limited totablets, capsules and microbeads, preferably sugar beadlets ormicrocrystalline cellulose.

For oral administration, the components of the composition may beincorporated into a tablet, aqueous or oil suspension, dispersiblepowder or granule, microbead, emulsion, hard or soft capsule, syrup orelixir. These components may also be administered separately.Compositions may be prepared according to any method known in the artfor the manufacture of pharmaceutically acceptable compositions and suchcompositions may contain one or more of the following agents:sweeteners, flavoring agents, coloring agents and preservatives. Tabletscontaining the active ingredients in admixture with non-toxicpharmaceutically acceptable excipients suitable for tablet manufactureare acceptable. “Pharmaceutically acceptable” means that the agentshould be acceptable in the sense of being compatible with the otheringredients of the formulation (as well as non-injurious to theindividual). Such excipients include inert diluents such as calciumcarbonate, sodium carbonate, lactose, calcium phosphate or sodiumphosphate; granulating and disintegrating agents, such as corn starchand alginic acid; binding agents such as starch, gelatin or acacia; andlubricating agents such as magnesium stearate, stearic acid or talc.Tablets may be uncoated or may be coated with known techniques to delaydisintegration and absorption in the gastrointestinal tract and therebyprovide a sustained action over a longer period of time. For example, atime delay material such as glyceryl monostearate or glyceryl stearatealone or with a wax may be employed.

Another embodiment of the present invention is a pharmaceuticalcomposition comprising an enteric-coated chromic tripicolinate orchromic polynicotinate formulation. Any pharmaceutical formulation wellknown in the art can be coated with an enteric coating. In a preferredembodiment, the formulation is a tablet, capsule or microbead, either inthe presence or absence of at least one of a cox inhibitor, acid,mucolytic and salicin-containing herb.

Formulations for oral use may also be presented as hard gelatin capsuleswherein the active ingredient is mixed with an inert solid diluent, forexample calcium carbonate, calcium phosphate or kaolin, or as softgelatin capsules wherein the active ingredient is mixed with water or anoil medium, such as peanut oil, liquid paraffin or olive oil.

Aqueous suspensions may contain the chromic tripicolinate orpolynicotinate compositions of the invention in admixture withexcipients for the manufacture of aqueous suspensions. Such excipientsinclude suspending agents, dispersing or wetting agents, one or morepreservatives, one or more coloring agents, one or more flavoring agentsand one or more sweetening agents such as sucrose or saccharin.

Oil suspensions may be formulated by suspending the active ingredient ina vegetable oil, such as arachis oil, olive oil, sesame oil or coconutoil, or in a mineral oil such as liquid paraffin. The oil suspension maycontain a thickening agent, such as beeswax, hard paraffin or cetylalcohol. Sweetening agent, such as those set forth above, and flavoringagents may be added to provide a palatable oral preparation. Thesecompositions may be preserved by an added antioxidant such as ascorbicacid. Dispersible powders and granules of the invention suitable forpreparation of an aqueous suspension by the addition of water providethe active ingredient in admixture with a dispersing or wetting agent, asuspending agent, and one or more preservatives. Additional excipients,for example sweetening, flavoring and coloring agents, may also bepresent.

Syrups and elixirs may be formulated with sweetening agents, such asglycerol, sorbitol or sucrose. Such formulations may also contain ademulcent, a preservative, a flavoring or a coloring agent.

In a preferred embodiment, the components of the composition are coatedonto microbeads. In a preferred embodiment, these microbeads are sugarbeadlets of various sizes, also known as nonpareils, and arecommercially available from, for example, SmithKline Beecham. If themicrobeads are to be used to administer the compositions of theinvention to diabetic patients, the administration of other types ofmicrobeads, such as microcrystalline cellulose, is preferred.Microcrystalline cellulose is commercially available and can beprocessed into beadlets of various sizes by micronization, a techniquewell known in the art. The microbeads are essentially a carrier for thecompositions of the invention. For a description of coated beadlets,see, for example, Carstensen, J. T., Pharmaceutical Principles of solidDosage Forms, Technonic Publishing Co., Inc., Lancaster, Pa., pp.228-230, 1993, hereby incorporated by reference. Aqueous solutionscontaining the chromic tripicolinate or chromic polynicotinate andnicotinic acid and/or picolinic acid components of the composition aresprayed onto the microbeads by well known methods, by suspending themicrobeads in an upcurrent of air and introducing a fine spray of theactive ingredients which form a coating on the outside of the microbeadswhich is then allowed to dry. The desired components (e.g. chromictripicolinate and ibuprofen) may be combined into the same solution orapplied using separate solutions. Optionally, the coated microbeads canbe further coated with a substance to protect the active ingredientscoated onto the beads, such as latex. The microbeads may be placed in acapsule prior to administration. In another preferred embodiment, thecapsule or the microbeads are coated with an enteric coating to delaydissolution until reaching the small intestine.

Typically, the chromic tripicolinate and chromic polynicotinatecompositions of the invention provide between about 50 and 10,000micrograms per day of chromium; preferably between about 100 and 2,000micrograms per day; more preferably, between about 200 and 1,000micrograms per day.

It will be appreciated that although specific embodiments of theinvention have been described herein for purposes of illustration,various modifications may be made without deviating from the spirit andscope of the invention. Accordingly, the invention is not limited exceptas by the appended claims.

What is claimed is:
 1. A composition for supplementing dietary chromiumand facilitating absorption of essential metals, said compositioncomprising chromium polynicotinate in combination with a cyclooxygenaseinhibitor other than acetylsalicylic acid, wherein said composition isnot enteric coated.
 2. The composition of claim 1, wherein saidcomposition is in the form of a tablet, capsule or microbead.
 3. Thecomposition of claim 2, wherein the microbead is a sugar beadlet ormicrocrystalline cellulose beadlet and said composition is coated onsaid beadlet.
 4. The composition of claim 1, wherein said cyclooxygenaseinhibitor is indomethacin.
 5. The composition of claim 1, wherein saidcyclooxygenase inhibitor is ibuprofen.
 6. The composition of claim 1,wherein said cyclooxygenase inhibitor is acetaminophen.
 7. Thecomposition of claim 1, wherein said cyclooxygenase inhibitor isnaproxen.
 8. A composition for supplementing dietary chromium andfacilitating absorption of essential metals, said composition comprisingchromium polynicotinate in combination with an acid other thanacetylsalicylic acid, wherein said composition is not enteric coated. 9.The composition of claim 8, wherein said acid is ascorbic acid or citricacid.
 10. A composition for supplementing dietary chromium andfacilitating absorption of essential metals, said composition comprisingchromium polynicotinate in combination with a mucolytic, wherein saidcomposition is not enteric coated.
 11. The composition of claim 10,wherein said mucolytic is guaifenesin.
 12. A composition forsupplementing dietary chromium and facilitating absorption of essentialmetals, said composition comprising chromium polynicotinate incombination with a salicin-containing herb, wherein said composition isnot enteric coated.
 13. The composition of claim 12, wherein saidsalicin-containing herb is selected from the group consisting ofBoswellia serrata (frankincense), Betula lenta (sweet birch), Betulapubescens (white birch), Filipendula ulmaria (meadowsweet), Gaultheriaprocumbens (wintergreens), Populus balsamifera, Populus jackii (balm ofGilead) and Salix alba (white willow).
 14. A method for supplementingdietary chromium in an individual, comprising orally administering tosaid individual a composition comprising chromium polynicotinate incombination with a cyclooxygenase inhibitor other than acetylsalicylicacid, wherein said composition is not enteric coated.
 15. The method ofclaim 14, wherein said composition is in the form of a tablet, capsuleor microbead.
 16. The method of claim 15, wherein the microbead is asugar beadlet or microcrystalline cellulose beadlet and said compositionis coated on said beadlet.
 17. A method for reducing hyperglycemia andstabilizing serum glucose levels in an individual in need thereof,comprising orally administering to said individual a compositioncomprising chromium polynicotinate in combination with a cyclooxygenaseinhibitor other than acetylsalicylic acid, wherein said composition isnot enteric coated.
 18. The method of claim 17, wherein said compositionis in the form of a tablet, capsule or microbead.
 19. The method ofclaim 18, wherein said microbead is a sugar beadlet or microcrystallinecellulose beadlet and said composition is coated on said beadlet.
 20. Amethod for increasing lean body mass and reducing body fat of anindividual in need thereof, comprising orally administering to saidindividual a composition comprising chromium polynicotinate incombination with a cyclooxygenase inhibitor other than acetylsalicylicacid, wherein said composition is not enteric coated.
 21. The method ofclaim 20, wherein said composition is in the form of a tablet, capsuleor microbead.
 22. The method of claim 21, wherein said microbead is asugar beadlet or microcrystalline cellulose beadlet and said compositionis coated on said beadlet.
 23. A method for reducing high levels ofblood serum lipids in an individual in need thereof, comprisingadministering to said individual a composition comprising chromiumpolynicotinate in combination with a cyclooxygenase inhibitor other thanacetylsalicylic acid, wherein said composition is not enteric coated.24. The method of claim 23, wherein said composition is in the form of atablet, capsule or microbead.
 25. The method of claim 24, wherein saidmicrobead is a sugar beadlet or microcrystalline cellulose beadlet andsaid composition is coated on said beadlet.
 26. A method forsupplementing dietary chromium in an individual, comprising orallyadministering to said individual a composition comprising chromiumpolynicotinate in combination with an acid other than acetylsalicylicacid, wherein said composition is not enteric coated.
 27. The method ofclaim 26, wherein said acid is selected from the group consisting ofascorbic acid and citric acid.
 28. A method for supplementing dietarychromium in an individual, comprising orally administering to saidindividual a composition comprising chromium polynicotinate incombination with a mucolytic, wherein said composition is not entericcoated.
 29. The method of claim 28, wherein said mucolytic isguaifenesin.
 30. A method for supplementing dietary chromium in anindividual, comprising orally administering to said individual acomposition comprising chromium polynicotinate in combination with asalicin-containing herb, wherein said composition is not enteric coated.31. The method of claim 30, wherein said salicin-containing herb isselected from the group consisting of Boswellia serrata (frankincense),Betula lenta (sweet birch), Betula pubescens (white birch), Filipendulaulmaria (meadowsweet), Gaultheria procumbens (wintergreens), Populusbalsamifera, Populus jackii (balm of Gilead) and Salix alba (whitewillow).
 32. A method for reducing hyperglycemia and stabilizing serumglucose levels in an individual in need thereof, comprising orallyadministering to said individual a composition comprising chromiumpolynicotinate in combination with an acid other than acetylsalicylicacid, wherein said composition is not enteric coated.
 33. The method ofclaim 32, wherein said acid is selected from the group consisting ofascorbic acid and citric acid.
 34. A method for reducing hyperglycemiaand stabilizing serum glucose levels in an individual in need thereof,comprising orally administering to said individual a compositioncomprising chromium polynicotinate in combination with a mucolytic,wherein said composition is not enteric coated.
 35. The method of claim34, wherein said mucolytic is guaifenesin.
 36. A method for reducinghyperglycemia and stabilizing serum glucose levels in an individual inneed thereof, comprising orally administering to said individual acomposition comprising chromium polynicotinate in combination with asalicin-containing herb, wherein said composition is not enteric coated.37. The method of claim 36, wherein said salicin-containing herb isselected from the group consisting of Boswellia serrata (frankincense),Betula lenta (sweet birch), Betula pubescens (white birch), Filipendulaulmaria (meadowsweet), Gaultheria procumbens (wintergreens), Populusbalsamifera, Populus jackii (balm of Gilead) and Salix alba (whitewillow).
 38. A method for increasing lean body mass and reducing bodyfat of an individual in need thereof, comprising orally administering tosaid individual a composition comprising chromium polynicotinate incombination with an acid other than acetylsalicylic acid, wherein saidcomposition is not enteric coated.
 39. The method of claim 38, whereinsaid acid is selected from the group consisting of ascorbic acid andcitric acid.
 40. A method for increasing lean body mass and reducingbody fat of an individual in need thereof, comprising orallyadministering to said individual a composition comprising chromiumpolynicotinate in combination with a mucolytic, wherein said compositionis not enteric coated.
 41. The method of claim 40, wherein saidmucolytic is guaifenesin.
 42. A method for increasing lean body mass andreducing body fat of an individual in need thereof, comprising orallyadministering to said individual a composition comprising chromiumpolynicotinate in combination with a salicin-containing herb, whereinsaid composition is not enteric coated.
 43. The method of claim 42wherein said salicin-containing herb is selected from the groupconsisting of Boswellia serrata (frankincense), Betula lenta (sweetbirch), Betula pubescens (white birch), Filipendula ulmaria(meadowsweet), Gaultheria procumbens (wintergreens), Populusbalsamifera, Populus jackii (balm of Gilead) and Salix alba (whitewillow).
 44. A method for reducing high levels of blood serum lipids inan individual in need thereof, comprising orally administering to saidindividual a composition comprising chromium polynicotinate incombination with an acid other than acetylsalicylic acid, wherein saidcomposition is not enteric coated.
 45. The method of claim 44, whereinsaid acid is selected from the group consisting of ascorbic acid andcitric acid.
 46. A method for reducing high levels of blood serum lipidsin an individual in need thereof, comprising orally administering tosaid individual a composition comprising chromium polynicotinate incombination with a mucolytic, wherein said composition is not entericcoated.
 47. The method of claim 46, wherein said mucolytic isguaifenesin.
 48. A method for reducing high levels of blood serum lipidsin an individual in need thereof, comprising orally administering tosaid individual a composition comprising chromium polynicotinate incombination with a salicin-containing herb, wherein said composition isnot enteric coated.
 49. The method of claim 48 wherein saidsalicin-containing herb is selected from the group consisting ofBoswellia serrata (frankincense), Betula lenta (sweet birch), Betulapubescens (white birch), Filipendula ulmaria (meadowsweet), Gaultheriaprocumbens (wintergreens), Populus balsamifera, Populus jackii (balm ofGilead) and Salix alba (white willow).